RS1064797327 LAMA2
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What This Variant Does
"CLNSIG=4
Associated Conditions
LAMA2-related muscular dystrophy
Merosin deficient congenital muscular dystrophy
LAMA2-related muscular dystrophy
LAMA2-related muscular dystrophy
Merosin deficient congenital muscular dystrophy
LAMA2-related muscular dystrophy
Other Variants in LAMA2